Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Thrombocytopenia

A reduction in the number of circulating thrombocytes.


Total: 3

                       


(per page)
PMID (PMCID)
25908903
(4381885)
 OTHER
Thrombocytopenia absent radius syndrome with Tetralogy of Fallot: a rare association.
Kumar C, Sharma D, Pandita A, Bhalerao S.
Int Med Case Rep J. 2015;8:81-5.
The patient was diagnosed to have Tetralogy of Fallot, for which the infant was managed with definitive repair and thrombocytopenia was managed with platelet transfusion.
17541300
 MALE Infant
Chromosome 22q11.2 deletion presenting with immune-mediated cytopenias, macrothrombocytopenia and platelet dysfunction.
Akar NA, Adekile AD.
Med Princ Pract. 2007;16(4):318-20.
The patient presented in the neonatal period with tetralogy of Fallot, subtle dysmorphic features and thrombocytopenia.
9597899
 MALE Adult
[Hereditary macrothrombocytopenia].
Kasahara K, Takahashi T, Hamamoto F, Hayashi T, Adachi M, Okuda H, Satoh S, Hinoda Y, Imai K.
Rinsho Ketsueki. 1998;39(4):308-13.
When he underwent a shunt operation for tetralogy of Fallot without any complication at nine-years old, thrombocytopenia was allegedly pointed out for the first time.